Canonical Allele Identifier: PA2741819648
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2789216
ClinVar RCV Id: RCV003633901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000630.1:p.Met213Ile
CA1247598
NM_000639.3:c.639G>A
CA343806293
NM_000639.3:c.639G>C
CA343806294
NM_000639.3:c.639G>T